🛠 Tech Stack

💼 About This Role

You'll join a sponsor-dedicated team within a global CRO, managing clinical trials in dermatology. Your core impact includes ensuring site compliance with GCP/ICH guidelines and delivering high-quality data. This role offers the security of a large CRO with the focus of a single sponsor.

🎯 What You'll Do

• Conduct site evaluation, initiation, and monitoring visits
• Review Case Report Forms for accuracy and completeness
• Perform source data verification and resolve data queries
• Train site staff on study procedures

📋 Requirements

• University degree in scientific, medical, or paramedical discipline
• Proven experience as a CRA with on-site monitoring activities
• Previous experience in dermatology studies
• Strong knowledge of GCP/ICH Guidelines and regulatory requirements

✨ Nice to Have

• Experience with contract negotiation
• Familiarity with submission processes

🎁 Benefits & Perks

• 🔒 Career security with a global CRO
• 📚 Continuous training and professional development
• 🌍 Opportunity to work across multiple countries
• 🤝 Supportive culture with below-industry turnover

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Submit CV· 1 day
2. 2Phone interview· 30 min
3. 3Offer· 1 week